Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs398123007
rs398123007
Entrez Id: 9897
Gene Symbol: WASHC5
WASHC5
CUI: C4551776
Disease:
RITSCHER-SCHINZEL SYNDROME 1
T 0.700 CausalMutation CLINVAR